@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP577881.RAgmEnj00eP45ljO0yRmOCYNtgwZX9oFdwwWMpJuzujgA
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
@prefix lld: <
http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP577881.RAgmEnj00eP45ljO0yRmOCYNtgwZX9oFdwwWMpJuzujgA130_head
{
this:
np:hasAssertion
dgn-np:NP577881.RAgmEnj00eP45ljO0yRmOCYNtgwZX9oFdwwWMpJuzujgA130_assertion
;
np:hasProvenance
dgn-np:NP577881.RAgmEnj00eP45ljO0yRmOCYNtgwZX9oFdwwWMpJuzujgA130_provenance
;
np:hasPublicationInfo
dgn-np:NP577881.RAgmEnj00eP45ljO0yRmOCYNtgwZX9oFdwwWMpJuzujgA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP577881.RAgmEnj00eP45ljO0yRmOCYNtgwZX9oFdwwWMpJuzujgA130_assertion
a
np:Assertion
.
dgn-np:NP577881.RAgmEnj00eP45ljO0yRmOCYNtgwZX9oFdwwWMpJuzujgA130_provenance
a
np:Provenance
.
dgn-np:NP577881.RAgmEnj00eP45ljO0yRmOCYNtgwZX9oFdwwWMpJuzujgA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP577881.RAgmEnj00eP45ljO0yRmOCYNtgwZX9oFdwwWMpJuzujgA130_assertion
{
miriam-gene:8036
a
ncit:C16612
.
lld:C0028326
a
ncit:C7057
.
dgn-gda:DGN047b8b9e39d739339610f2ab873bb030
sio:SIO_000628
miriam-gene:8036
,
lld:C0028326
;
a
sio:SIO_001121
.
}
dgn-np:NP577881.RAgmEnj00eP45ljO0yRmOCYNtgwZX9oFdwwWMpJuzujgA130_provenance
{
dgn-np:NP577881.RAgmEnj00eP45ljO0yRmOCYNtgwZX9oFdwwWMpJuzujgA130_assertion
dcterms:description
"[Germline mutations in genes encoding small GTPases of the RAS family (KRAS and NRAS), modulators of RAS function (PTPN11, SOS1 and SHOC2) or downstream signal transducers (RAF1) are causative for NS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
;
sio:SIO_000772
miriam-pubmed:20673819
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
xsd:date
.
dgn-void:source_evidence_literature
a
eco:ECO_0000212
;
rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
"DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP577881.RAgmEnj00eP45ljO0yRmOCYNtgwZX9oFdwwWMpJuzujgA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:48+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}